Variant (rsID / SNP)

rs2775254

rs2775254 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR4L1. Location: chromosome 14, position 20,528,528. The table records no clinical significance for this variant.

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Reference-table entries

OR4L1Not classified

Variant type: missense_variant
Chromosome / position: 14:20528528
HGVS: NM_001004717.1,c.325G>A,p.Gly109Ser
Allele change: Missense_G109S

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.